Evaluation of transforming growth factor-beta 1 level in crevicular fluid of cyclosporin A-treated patients

Citation
N. Buduneli et al., Evaluation of transforming growth factor-beta 1 level in crevicular fluid of cyclosporin A-treated patients, J PERIODONT, 72(4), 2001, pp. 526-531
Citations number
40
Categorie Soggetti
Dentistry/Oral Surgery & Medicine","da verificare
Journal title
JOURNAL OF PERIODONTOLOGY
ISSN journal
00223492 → ACNP
Volume
72
Issue
4
Year of publication
2001
Pages
526 - 531
Database
ISI
SICI code
0022-3492(200104)72:4<526:EOTGF1>2.0.ZU;2-W
Abstract
Background: The aim of the present study was to investigate the level of tr ansforming growth factor-beta1 (TGF-beta1) in gingival crevicular fluid (GC F) samples of cyclosporin A (CsA)-treated patients and to compare the resul ts with control groups. Methods: Fourteen renal transplant patients exhibiting severe CsA-induced g ingival overgrowth, 10 patients with chronic gingivitis, and 10 subjects wi th clinically healthy periodontium were included in the study. In CsA-treat ed patients, GCF samples were harvested from sites exhibiting gingival over growth (CsA GO+) and sites not exhibiting gingival overgrowth (CsA GO-). Th e TGF-beta1 levels in a total of 96 GCF samples from the 34 participants we re analyzed by enzyme-linked immunosorbent assay. The results were expresse d in terms of total amount (pg/2 sites) and concentration (ng/ml). Results: TGF-beta1 total amounts in CsA GO+ and CsA GO-sites were similar a nd significantly higher than that of healthy sites (P <0.02 and P <0.01, re spectively). The total amount of TGF-beta1 was also higher in gingivitis si tes compared to the healthy sites, but the difference was not statistically significant (P >0.05). CsA GO+ and CsA GO- sites exhibited higher total am ount and concentration of TGF-beta1 than that of gingivitis sites, but the differences were insignificant (P >0.05). Conclusions: The results of the present study support the theory that CsA i ncreases the synthesis of TGF-beta1 in GCF However, since the difference be tween CsA GO+ and CsA GO- sites was not statistically significant, it seems unlikely that GCF TGF-beta1 level is the sole factor responsible for the C sA-induced gingival overgrowth. Complex interactions between various mediat ors of inflammation and tissue modeling are possibly involved in the pathog enic mechanisms of this side effect.